Gemini, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K810870 | GEMENI CK-MB ISOENZYME ABNORMAL SERUM | JJT | 1981-04-14 | View |
| 510(k) | K810534 | GEMENI QUICK-MB SEPARATION KIT | JHT | 1981-03-11 | View |
No matching devices.
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